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Gestational diabetes, atopic dermatitis, and allergen sensitization in early childhood
Rajesh Kumar1, Fengxiu Ouyang, Rachel E Story
1Division of Allergy and Immunology, Children's Memorial Hospital, Chicago, Ill 60614, USA. rkumar@childrensmemorial.org
Insights
Gestational diabetes (GDM) significantly increases the risk of atopic dermatitis and allergen sensitization in infants born at term. These risks are independent of maternal weight and fetal growth, highlighting GDM as a key prenatal factor for childhood allergies.
Area of Science:
- Perinatal Medicine
- Immunology
- Pediatric Allergy
Background:
- The prenatal environment's impact on offspring allergic disease is not fully understood.
- Maternal-fetal interactions during pregnancy require further investigation regarding allergy development.
Purpose of the Study:
- To investigate if gestational diabetes (GDM) influences the risk of atopic dermatitis and allergen sensitization in early childhood.
- To explore the association between GDM and specific atopic manifestations in offspring.
Main Methods:
- Prospective cohort study of 680 mother-child dyads from the Boston Birth Cohort.
- Assessed physician-diagnosed atopic dermatitis and allergen sensitization (food and aeroallergens) via ImmunoCAP.
- Analyzed GDM using medical record review and logistic regression, stratified by term/preterm birth, controlling for covariates.
Main Results:
- Gestational diabetes (GDM) was present in 4.9% of mothers.
- In term births, GDM was significantly associated with increased odds of atopic dermatitis (OR 7.2) and allergen sensitization (OR 5.7).
- Food sensitization drove the association with sensitization; no associations were found in preterm births.
Conclusions:
- Gestational diabetes mellitus (GDM) is linked to a higher risk of atopic dermatitis and early childhood allergen sensitization in term infants.
- These risks associated with GDM are independent of maternal prepregnancy BMI and fetal growth.
- Findings underscore the importance of managing GDM to potentially mitigate childhood allergic diseases.
Background:
The relationship between the prenatal environment, maternal-fetal interaction, and allergic disease in the offspring remains understudied.
Objective:
We sought to determine whether gestational diabetes (GDM) modifies the risk of early childhood atopic manifestations, including atopic dermatitis and allergen sensitization.
Methods:
This study includes 680 children from the Boston Birth Cohort. Mother-child dyads were recruited at birth and followed prospectively to a mean age of 3.2 +/- 2.3 years, with study visits aligned with the pediatric primary care schedule. The primary outcomes were physician-diagnosed atopic dermatitis on standardized medical record abstraction and allergen sensitization based on ImmunoCAP to 7 common foods and 5 common aeroallergens (specific IgE, >or=0.10 kUA/L; Phadia, Uppsala, Sweden). GDM was determined by means of standardized medical record review. Logistic regression analysis, stratified by term/preterm status, evaluated the association of GDM with atopic dermatitis and allergen sensitization, respectively, controlling for maternal prepregnancy body mass index, fetal growth, and pertinent covariates.
Results:
Of the 680 children, 488 were term, and 192 were preterm (<37 weeks' gestation). Overall, 4.9% of the mothers had GDM. Among the 680 children, 34.4% had atopic dermatitis, and 51% had allergen sensitization. In term births GDM was significantly associated with atopic dermatitis (odds ratio [OR], 7.2; 95% CI, 1.5-34.5) and allergen sensitization (OR, 5.7; 95% CI, 1.2-28.0). Adjusting for fetal growth had little effect. The association with sensitization was driven primarily by food sensitization (OR, 8.3; 95% CI, 1.6-43.3). The above associations were not observed in preterm births.
Conclusions:
In term births GDM increased the risk of atopic dermatitis and early childhood allergen sensitization independently of maternal prepregnancy body mass index and fetal growth.
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